4091-02-5

Basic information

• Product Name: vinyl methyl terephthalate
• Synonyms: vinyl methyl terephthalate
• CAS NO: 4091-02-5
• Molecular Weight: 206.198
• Mol File: 4091-02-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: vinyl methyl terephthalate(CAS DataBase Reference)
• NIST Chemistry Reference: vinyl methyl terephthalate(4091-02-5)
• EPA Substance Registry System: vinyl methyl terephthalate(4091-02-5)

Safety Data

• Hazardous Substances Data: 4091-02-5(Hazardous Substances Data)

Upstream product

• 108-05-4 vinyl acetate 
• 1679-64-7 Monomethyl terephthalate 
• 74-86-2 acetylene 

Downstream Products

• 7377-26-6 4-Methoxycarbonylbenzoyl chloride 
• 16210-30-3 Terephthalsaeure-methylester-<β-dichlorphosphoryl-vinylester> 
• 16209-94-2 Methyl-α,β-dibromaethyl-terephthalat 
• 16278-51-6 Methyl-α,β-dichloraethyl-terephthalat 
• 16278-32-3 Methyl-α-bromaethyl-terephthalat 
• 16210-23-4 Methyl-α-chloraethyl-terephthalat 

Relevant articles and documents

The Photocycloaddition of N-Vinylcarbazole with 3-Cyanostyrene

The photocycloaddition reaction of N-vinylcarbazole (VCZ) as an electron donor, with 3-cyanostyrene as an electron acceptor, was studied.In nonpolar solvents, two cyclobutanes of cis-1-(9-carbazolyl)-2-(3-cyanophenyl)cyclobutane and trans-1-(9-carbazolyl)-2-(3-cyanophenyl)cyclobutane (in a ratio of 3:1) were obtained from an exciplex intermediate.The structure of cis cyclobutane seemed to originate from a sandwich conformation of the exciplex.In polar solvents, a photodissociation to free ion radicals was observed and trans-1,2-di(9-carbazolyl)cyclobutane was produced efficiently by means of a chain mechanism via a cation radical of VCZ.Transient intermediates were measured by means of nanosecond laser photolysis; the results supported the reaction scheme.